Add genetic testing to your baby's health toolkit

Each year, an estimated 7.9 million babies worldwide are born with birth defects, many of which appear healthy at birth and come from families with no history of the disorder. Many affected babies are not identified until the appearance of severe and often irreversible symptoms later in life.

Detecting a disease at an early stage can enable appropriate and timely medical intervention before more serious and sometimes irreversible health issues are caused.

Why need genetic testing for newborns or children?

There are an estimated 300 000 infant deaths annually in the Pakistan. According to the most up-to-date data available, the neonatal mortality rate is 42 per 1000 live births,3 which accounts for almost 7% of all newborn deaths globally

Most of these neonates death is due to some inherited inborn error of metabolism or some genetic disorders

How testing works

Step 1
Request a test online. An independent clinician will review and approve your order.
Step 2
Provide a saliva sample from the comfort of your home and ship it to our lab.
Step 3
Get your results and share them with your doctor. If you'd like, talk to a genetic counselor at no extra cost.

Find the right test

Talk to us for finding out the right testing option for your child!